Научная статья на тему 'Origin and evolution of Paramecium bursaria / Chlorella symbiotic system: what can one say about the host evolution studying evolution of symbiont?'

Origin and evolution of Paramecium bursaria / Chlorella symbiotic system: what can one say about the host evolution studying evolution of symbiont? Текст научной статьи по специальности «Биологические науки»

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Текст научной работы на тему «Origin and evolution of Paramecium bursaria / Chlorella symbiotic system: what can one say about the host evolution studying evolution of symbiont?»

Protistology ■ 63

zerland

6 - Jardin Botanique de Neuchátel, Chemin du Per-thuis-du-Sault 58, CH-2000Neuchátel, Switzerland [email protected]

Hyalospheniids are among the most common and conspicuous testate amoebae in high-latitude peatlands and forest humus. These testate amoebae were widely studied as bioindicators, and are increasingly used as models in microbial biogeography. However, data on their diversity and ecology are still very unevenly distributed geographically: notably, data are lacking for low latitude peatlands. We describe here a new species, Nebela jiuhuensis, from peatlands near the Middle Yangtze River reach of south central China with characteristic morphology. The test (shell) has hollow horn-like lateral extensions also found in N. saccifera, N. equicalceus (=N. hippocrepis) and N. ansata, three large species restricted mostly to Sphagnum-peatlands of Eastern North America. Mitochondrial cytochrome oxidase (COI) data confirm that N. jiuhuensis is closely related to the morphologically very similar North American species N. saccifera and more distantly to N. ansata within the N. penardiana group. These species are all found in wet mosses growing in poor fens. Earlier re-ports ofmorphologically similar specimens found in South Korea peatlands suggest that N. jiuhuensis may be distributed in comparable peatlands in Eastern Asia (China and Korea). The discovery of such a conspicuous new species in Chinese peatlands suggests that many new testate amoebae species are yet to be discovered, including potential regional endemics. Furthermore, human activities (e.g. drainage, agriculture, pollution) have reduced the known habitat of N. jiuhuensis, which can thus be considered as locally endangered. We therefore suggest that this very conspicuous microorganism with a probably limited geographical distribution and specific habitat requirement should be considered as a flagship species for microbial biogeo-graphy as well as local environmental conservation and management. Key words: Arcellinid testate amoebae; biodiversity conservation; biogeography; DNA barcoding; mtCOI.

EPIBIONTIC RELATIONSHIP IN AN ARTIFICIAL POND OF CHIAPAS (MEXICO): PROCAMBARUS (AUSTROCAMBARUS) SP. (CRUSTACEA: DECAPODA) AND EPISTYLIS HENTSCHELI (CILIOPHORA: PERITRI-CHIA)

Ramírez-Ballesteros M.1, Fernandez-Leborans G.2, Mayén-Estrada R.3

1 - Laboratorio de Protozoología, Departamento de Biología Comparada, Facultad de Ciencias, Universidad Nacional Autónoma de México, Mexico

2 - Departamento de Zoología, Facultad de Biología, Universidad Complutense, Madrid, España

3 - Laboratorio de Protozoología, Departamento de Biología Comparada, Facultad de Ciencias, Universidad Nacional Autónoma de México, México [email protected]

Several samples collected during years 2014 and 2015 contained epibenthonic fauna with the crayfish Procambarus (Austrocambarus) sp. Samplings were performed on the freshwater artificial pond Yaleon, located in Montebello (Chiapas, SE Mexico), using a 5 mm opening hand net. The environment was strongly polluted with organic matter (assimilated to a polysaprobic zone). The crayfish Procambarus (Austrocambarus) sp. harbored colonies of a peri-trich ciliate identified as Epistylis hentscheli Kahl, 1935. This ciliate formed ramified colonies with a moderate number of zooids (up to 30). Stalks of the colony were dichotomously branched, and they presented peripherical fibres arranged longitudinally. The zooid was elongated; the form ofbody was similar to a bell (170-200 ^m in lenght), with a C-shaped transversal macronucleus, and a spherical micronucleus near to the macronucleus. The peristomal lip was very thin. The buccal infraciliature had the general pattern of peritrichids and was composed by a haplokinety and a polykinety drawing a spiral with 1.5 rounds inside the buccal infundibulum. These epibionts were located exclusively on the pereiopods. The goal of this contribution is to provide data about cell/colony structure of E. hentscheli and also its distribution on the crayfish. This is the first record ofthis epibiont peritrich ciliate on crustacea, being previously found on algae and fish. Acknowledgements: to Posgrado en Ciencias Biolygicas, Universidad Nacional Autónoma de México and CONACyT, for the support necessary for carry out this research. Additionally, we are indebted to Dr. Villalobos-Hiriart (Instituto de Biología, UNAM) for the crustacean identification and to Biol. Reyes-Santos (Facultad de Ciencias, UNAM) for their help with impregnation techniques. We also appreciate the technical support ofthe Department of Zoology (Universidad Complutense, UCM, España).

ORIGIN AND EVOLUTION OF PARAMECIUM BURSARIA / CHLORELLA SYMBIOTIC SYSTEM: WHAT CAN ONE SAY ABOUT THE HOST EVOLUTION STUDYING EVOLUTION OF SYMBIONT?

Rautian M., Beliavskaia A., Kiselev A. Saint Petersburg State University, Russia

64 • "PROTIST—2016

[email protected]

BACKGROUND. P. bursaria belongs to one of the best studied Ciliate's genus Paramecium. This species diverged basically from other paramecia. They possess symbiotic Chlorella in the cytoplasm. These Chlorella were attributed to three Chlorella species — Ch. vulgaris, Ch. variabilis and Micractinum reisseri according to their phylogeny inferred from ITS1-5.8S-ITS2-5'LSU rDNA sequence and their sensitivity to specific viruses (PBCV). Morphospecies P. bursaria consist of 5 syngens — reproductively isolated intraspecies groups. Previously we have shown that syngens were represented by different branches on phylogenetic trees. The purpose of our investigation was to study phylogeny of P. bursaria and their symbiotic Chlorella using the same set of strains collected in different geographic regions. RESULTS. Gene RuBisCo have been used as molecular marker for Chlorella phylogeny. The tree consists of three separate branches. Diversity in each branch is negligible. Our data support strong correspondence between P. bursaria syngens and branch of Chlorella, while weak correlation between Chlorella type and its geographic location. CONCLUSIONS. According to our results we have concluded that successful symbiosis between P. bursaria ancestor and Chlorella has been established at least three times. The last time it had been happened before syngens R1 and R2 have diverged. We propose the strategy of evolution and geographic dispersion of this symbiotic system. Scientific research was performed at the Center for Culturing Collection ofMicroorganisms and Center for Molecular and Cell Technologies of Research park of St. Petersburg State University. Supported by RFBR grant 13-04-01714.

THE PLASTID GENOME OF POLYTOMA UVELLA IS THE LARGEST KNOWN AMONG NON-PHOTOSYNTHETIC ALGAE Reves-Prieto A.12

1 - Biology Department. University of New Brunswick, Fredericton

2 - Integrated Microbiology Program. Canadian Institute for Advanced Research. [email protected]

The polyphyletic assembly Polytoma and the species of the genus Polytomella represent different lineages within the Order Chlamydomonadales (Chlorophyta) that lost photosynthesis independently. The Polytomella clade is one of the two known groups of plastid-bearing eukaryotes that have lost completely the plastid genome (ptDNA)

after the loss of photosynthesis. Before the present report it was unknown if the absence of genome in the Polytomella plastids was a shared condition with species of the Polytoma genus. We present here the ptDNA of Polytoma uvella UTEX 964, which is the largest (circa 230 Kb) reported among non-photosynthetic algae. The ptDNA of P. uvella has lost all genes related with the photosynthetic function and its residual coding capacity is similar to ptDNAs from distantly related colorless chlorophytes, such as the pathogens Prototheca and Helicosporidium. The gene repertoire of the P. uvella ptDNA comprises mostly transcription and translation players and just few conserved proteins (e.g., FtsH-like, Ycf1-like and ClpP). Regardless of the substantial gene loss, the P. uvella ptDNA shows evidence of expansion due to the accumulation ofintergenic short repeated sequences (average length of 2.9 Kb). It is plausible that recombination-based DNA repair mechanisms are responsible of the genomic expansion of the P. uvella ptDNA.

SELECTION AND CHARACTERIZATION OF SINGLE CHAIN VARIABLE FRAGMENT (SCFV) ANTIBODIES AGAINST PNEUMOCYSTIS JIROVECII FROM PHAGE DISPLAY LIBRARIES

Ribeiro Marta, Cardoso Fernando, Matos Olga Medical Parasitology Unit, Group of Opportunistic Protozoa/HIVand Other Protozoa, Global Health and Tropical Medicine, Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Portugal [email protected]

Pneumocystis pneumonia (PcP) is an infectious disease caused by Pneumocystisjirovecii, an atypical fungus. PcP remains a major cause of respiratory illness among immunosuppressed patients. Current PcP diagnosis is based on the detection of P. jirovecii in respiratory specimens, obtained by invasive methods such as bronchoalveolar lavage, followed by cytochemical staining, immunofluorescent staining with monoclonal antibodies (IF/Mab) or PCR. Therefore, the possibility of an early diagnostic method allowing the use of biological specimens obtained non-invasively, is highly desirable. Rapid diagnostic tests (RDTs) using gold nanoparticles (AuNPs) allow a more sensitive, fast and cheap diagnosis, to be used in developing countries. The goal of this work is to develop an immunochromatographic RDT for the detection of P. jirovecii in non-invasive specimens like serum. In this test, spherical AuNPs are conjugated with a multi-epitope synthetic recombinant antigen (msr) which will allow the detection of circulating anti-P.

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